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rs41555122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41555122(A;G)
Make rs41555122(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271282
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41555122
dbSNP (old)rs41555122
ClinGenrs41555122
ebirs41555122
HLIrs41555122
Exacrs41555122
Gnomadrs41555122
Varsomers41555122
Maprs41555122
PheGenIrs41555122
Biobankrs41555122
1000 genomesrs41555122
hgdprs41555122
ensemblrs41555122
gopubmedrs41555122
geneviewrs41555122
scholarrs41555122
googlers41555122
pharmgkbrs41555122
gwascentralrs41555122
openSNPrs41555122
23andMers41555122
23andMe allrs41555122
SNP Nexus

SNPshotrs41555122
SNPdbers41555122
MSV3drs41555122
GWAS Ctlgrs41555122
Max Magnitude0
ClinVar
Risk rs41555122(G;G) rs41555122(T;T)
Alt rs41555122(G;G) rs41555122(T;T)
Reference Rs41555122(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239059T>A; NC_000006.11:g.31239059T>C
CLNSRC
CLNACC